Have questions? Visit https://www.reddit.com/r/SNPedia

rs587778944

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778944(-;-)
Make rs587778944(-;A)
Make rs587778944(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position36996677
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778944
ebirs587778944
HLIrs587778944
Exacrs587778944
Varsomers587778944
Maprs587778944
PheGenIrs587778944
hapmaprs587778944
1000 genomesrs587778944
hgdprs587778944
ensemblrs587778944
gopubmedrs587778944
geneviewrs587778944
scholarrs587778944
googlers587778944
pharmgkbrs587778944
gwascentralrs587778944
openSNPrs587778944
23andMers587778944
23andMe allrs587778944
SNP Nexus

SNPshotrs587778944
SNPdbers587778944
MSV3drs587778944
GWAS Ctlgrs587778944
Max Magnitude0
ClinVar
Risk rs587778944(A;A)
Alt rs587778944(A;A)
Reference rs587778944(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038168dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075356.2,